Sexton C J, Williams A T, Topley P, Shaw R J, Lovegrove C, Leigh I, Stables J N
Glaxo-Wellcome Research Laboratories, Beckenham, Kent, UK.
J Gen Virol. 1995 Dec;76 ( Pt 12):3107-12. doi: 10.1099/0022-1317-76-12-3107.
Human papillomaviruses (HPVs) are important human pathogens associated with a range of epithelial neoplasia. The rising incidence of HPV infection and association of HPV with malignancy has led to increased interest in appropriate management of these infections. Development of new therapies for viral warts has been frustrated by the lack of availability of models permissive for viral replication. Here we describe the development of HPV-severe combined immunodeficient mouse model which reproduces mature HPV-infected epithelia. Grafting of anogenital and laryngeal papillomas harbouring either HPV-6 or HPV-11 resulted in the formation of a differentiated neo-epithelium exhibiting the hallmark features of HPV infection including basal hyperplasia, acanthosis and koilocytosis. The reformed warty epithelium contained amplified HPV DNA and expressed capsid protein in the differentiated layers. A striking feature is the production of macroscopic papillomata in an anatomically relevant and accessible site, providing a system of particular relevance for the temporal evaluation of developing lesions and selection of antiviral agents.
人乳头瘤病毒(HPV)是与一系列上皮肿瘤相关的重要人类病原体。HPV感染发病率的上升以及HPV与恶性肿瘤的关联,使得人们对这些感染的适当管理越来越感兴趣。由于缺乏允许病毒复制的模型,病毒性疣新疗法的开发受到了阻碍。在此,我们描述了一种HPV - 严重联合免疫缺陷小鼠模型的开发,该模型可再现成熟的HPV感染上皮。移植携带HPV - 6或HPV - 11的肛门生殖器和喉乳头状瘤,会形成分化的新上皮,表现出HPV感染的标志性特征,包括基底增生、棘层肥厚和空泡化细胞。重新形成的疣状上皮含有扩增的HPV DNA,并在分化层中表达衣壳蛋白。一个显著特征是在解剖学相关且可触及的部位产生肉眼可见的乳头瘤,为发育中病变的时间评估和抗病毒药物的选择提供了一个特别相关的系统。